01 1Cambrex Profarmaco Milano S. r. l.
02 1F. I. S. Fabrica Italiana Sintetici S. p. A.
01 2Diazepam
01 1Italy
02 1U.S.A
Registration Number : 218MF10146
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2006-01-31
Latest Date of Registration : 2018-12-11
Registration Number : 217MF10542
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2022-12-23
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PharmaCompass offers a list of Diazepam API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Diazepam manufacturer or Diazepam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Diazepam manufacturer or Diazepam supplier.
PharmaCompass also assists you with knowing the Diazepam API Price utilized in the formulation of products. Diazepam API Price is not always fixed or binding as the Diazepam Price is obtained through a variety of data sources. The Diazepam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Relanium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Relanium, including repackagers and relabelers. The FDA regulates Relanium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Relanium API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Relanium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Relanium supplier is an individual or a company that provides Relanium active pharmaceutical ingredient (API) or Relanium finished formulations upon request. The Relanium suppliers may include Relanium API manufacturers, exporters, distributors and traders.
click here to find a list of Relanium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Relanium Drug Master File in Japan (Relanium JDMF) empowers Relanium API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Relanium JDMF during the approval evaluation for pharmaceutical products. At the time of Relanium JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Relanium suppliers with JDMF on PharmaCompass.
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